A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153



Internal ID15197897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2436746..2488309hg18UCSC Ensembl
Outerchr1:2479048..2530611hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg1851564
hg1751564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7171
Supporting Variants
SamplesNA19240
Known GenesHES5, LOC100133445, LOC115110, PANK4, TNFRSF14
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv1153
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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